CA2703021A1 - Catalyst composition and process for oligomerization of ethylene - Google Patents
Catalyst composition and process for oligomerization of ethylene Download PDFInfo
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- CA2703021A1 CA2703021A1 CA2703021A CA2703021A CA2703021A1 CA 2703021 A1 CA2703021 A1 CA 2703021A1 CA 2703021 A CA2703021 A CA 2703021A CA 2703021 A CA2703021 A CA 2703021A CA 2703021 A1 CA2703021 A1 CA 2703021A1
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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/189—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms containing both nitrogen and phosphorus as complexing atoms, including e.g. phosphino moieties, in one at least bidentate or bridging ligand
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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
- B01J31/143—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
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- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
- B01J31/1875—Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
- B01J31/188—Amide derivatives thereof
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- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
- C07C2/26—Catalytic processes with hydrides or organic compounds
- C07C2/36—Catalytic processes with hydrides or organic compounds as phosphines, arsines, stilbines or bismuthines
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- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/20—Olefin oligomerisation or telomerisation
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- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0238—Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
- B01J2531/0258—Flexible ligands, e.g. mainly sp3-carbon framework as exemplified by the "tedicyp" ligand, i.e. cis-cis-cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane
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- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/62—Chromium
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
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Abstract
The present invention relates to a catalyst composition comprising: (a) a binuclear chromium(II) complex; (b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, wherein R1, R2, R3, R4, R5, R6 and R7 are independently selected from halogen, amino, trimethylsilyl, C1-C10-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system; and (c) an activator or co-catalyst, as well as to a process for oligomerization of ethylene.
Description
Catalyst composition and process for oligomerization of ethylene The present invention relates to a catalyst composition and a process for the oligomerization of ethylene.
Linear alpha-olefins (LAOs) are very useful intermediates for the manufacture of detergents, synthetic lubricants, co-polymers, plasticizer alcohols and many other important products.
There are several producers of such LAOs via oligomerization of ethylene, e.g.
SHELL, BP, SABIC, AMOCO, CHEVRON PHILIPS etc.. An intrinsic problem of all of these metal-catalyzed ethylene oligomerization processes is the production of LAO mixtures following a mathematical distribution (Schulz-Flory or Poisson), which is difficult to separate and whose composition often does not match market demands. To solve this technical and economical unsatisfying situation, there is a deep interest to overcome the technical limitations and to transform the non-selective ethylene oligomerization reactions into more selective processes.
Recently these activities are predominantly concentrated on the selective trimerization of eth-ylene to 1-hexene (review: D.H. Morgan et al. J. Organomet. Chem. 2004, 689, 3641; and refs. Cited therein) as well as the selective tetramerization of ethylene to 1-octene (recent re-view: D. Wass, Dalton Trans. 2007, 816).
Several patents for the trimerization of ethylene to 1-hexene and the tetramerization of ethyl-ene to 1-octene are already known. In most of these cases different chromium precatalysts in combination with a broad array of different ligand systems and activating agents (like main group metal alkyl compounds) were utilized.
Prior art chromium based ethylene trimerization catalyst with chromium compounds, or-ganoaluminum activators and different ligands are those listed e.g. in the following patent publications: US Patent 4,668,838; EP 0 668 105; US Patent 5,750,817; US
Patent 6,031,145;
US Patent 5,811,681; EP 537609; EP 1574492; US 2004783429; WO 2005039758; FR
2833191; US 2002035029; WO 2002004119; WO 2001083447 and EP 1110930. Here, vari-ous chelating and non-chelating donor ligands and a large number of Cr(III) precursor com-pleses were claimed. In WO 2003004158, Cr(II) complexes such as chromium(II)acetate were
Linear alpha-olefins (LAOs) are very useful intermediates for the manufacture of detergents, synthetic lubricants, co-polymers, plasticizer alcohols and many other important products.
There are several producers of such LAOs via oligomerization of ethylene, e.g.
SHELL, BP, SABIC, AMOCO, CHEVRON PHILIPS etc.. An intrinsic problem of all of these metal-catalyzed ethylene oligomerization processes is the production of LAO mixtures following a mathematical distribution (Schulz-Flory or Poisson), which is difficult to separate and whose composition often does not match market demands. To solve this technical and economical unsatisfying situation, there is a deep interest to overcome the technical limitations and to transform the non-selective ethylene oligomerization reactions into more selective processes.
Recently these activities are predominantly concentrated on the selective trimerization of eth-ylene to 1-hexene (review: D.H. Morgan et al. J. Organomet. Chem. 2004, 689, 3641; and refs. Cited therein) as well as the selective tetramerization of ethylene to 1-octene (recent re-view: D. Wass, Dalton Trans. 2007, 816).
Several patents for the trimerization of ethylene to 1-hexene and the tetramerization of ethyl-ene to 1-octene are already known. In most of these cases different chromium precatalysts in combination with a broad array of different ligand systems and activating agents (like main group metal alkyl compounds) were utilized.
Prior art chromium based ethylene trimerization catalyst with chromium compounds, or-ganoaluminum activators and different ligands are those listed e.g. in the following patent publications: US Patent 4,668,838; EP 0 668 105; US Patent 5,750,817; US
Patent 6,031,145;
US Patent 5,811,681; EP 537609; EP 1574492; US 2004783429; WO 2005039758; FR
2833191; US 2002035029; WO 2002004119; WO 2001083447 and EP 1110930. Here, vari-ous chelating and non-chelating donor ligands and a large number of Cr(III) precursor com-pleses were claimed. In WO 2003004158, Cr(II) complexes such as chromium(II)acetate were
-2-claimed in conjunction with substituted cyclopentadienes as suitable ligand systems, in addi-tion to the already described and utilized Cr(III) complexes. In WO
2003053891, also Cr(II) complexes such as, e.g., chromium(II)acetate are claimed. The claimed ligands are bis(2-diphenylphosphino-ethyl)amines and derivatives thereof.
Prior art ethylene tetramerization catalysts include a number of different transition metal compounds, organoaluminum activators or different ligands, that have been used in the same or slightly modified form for the trimerization process. Patents concerning the tetramerization are: US Patent No. 6,184,428; US Patent No. 3,676,523; DE Patent 14 43 927; US
Patent No.
2003053891, also Cr(II) complexes such as, e.g., chromium(II)acetate are claimed. The claimed ligands are bis(2-diphenylphosphino-ethyl)amines and derivatives thereof.
Prior art ethylene tetramerization catalysts include a number of different transition metal compounds, organoaluminum activators or different ligands, that have been used in the same or slightly modified form for the trimerization process. Patents concerning the tetramerization are: US Patent No. 6,184,428; US Patent No. 3,676,523; DE Patent 14 43 927; US
Patent No.
3,906,053; WO 2005/086251; WO 2006108803, WO 2006099053, WO 2007057455, WO
2007057458 and WO 2007088329. In most of these patents, the obtained mixture of olefins does not contain more than 25 weight-% 1-octene. In some of the most recent applications, different PNP- and similar chelating donor ligands were claimed in conjunction with Cr(III) complexes only (WO 2004/056478 and WO 2004/056479). These applications were the first to demonstrate that in ethylene oligomerization a high selectivity towards 1-octene (up to 70 mass-%) with significantly less simultaneous 1-hexene production can be achieved. It was pointed out that the formed nine-membered ring systems (chromacyclononane) are the reason for the selective tetramerization of ethylene to 1-octene with 70% mass selectivity.
The selective ethylene trimerization and tetramerization catalysts and processes known gener-ally have to cope with some disadvantages. The catalysts show only low selectivities to the desired products 1-hexene and/or 1-octene due to by-products from side reaction channels.
Further limited purities of the products are obtained, i.e. the selectivities within the specific C6- or Cg-cut due to isomerization, branched olefin formation, etc.. Also wax formation, i.e.
formation of heavy, long-chain, high carbon-number products is detected. This is also true for polymer formation (polyethylene, branched and/or cross-linked polyethylene) leading to con-siderable product yield loss and fouling of equipment. Further it has to be mentioned that prior art processes only show poor turnover rates and catalyst activity resulted in high cost per kg product. Prior art catalysts and ligands are usually to be prepared with high costs. Ligands are usually difficult to synthesize, resulting in poor availability and high catalyst cost. The catalyst performance is highly susceptible to trace impurities, and the catalyst components are often difficult to handle in technical environment. The prior art processes usually require harsh reaction conditions, i.e. high temperatures and pressures, resulting in high invest, main-tenance and energy costs. Finally, high costs are also to be expected for co-catalyst/activator.
It is therefore an object of the present invention to overcome the difficulties of the prior art and to provide a catalyst composition showing improved selectivities and purities in the oli-gomerization of ethylene without formation of wax or polymer, showing rather improved turnover rates with fair costs for preparing catalyst and ligand.
Additionally, a process for the oligomerization of ethylene shall be provided.
The first object is achieved by a catalyst composition comprising: (a) a binuclear chro-mium(II) complex; (b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, wherein R1, R2, R3, R4, R5, R6 and R7 are independ-ently selected from halogen, amino, trimethylsilyl, C1-Clo-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system; and (c) an activator or co-catalyst.
As is to be understood, any cyclic derivatives of (A) and (B) can be utilized as ligand, wherein at least one of the P or N atoms of the PNPN-unit (structure (A)) or PNPNP-unit (structure (B)) is a ring member, the ring being formed from one or more constituent com-pounds of structures (A) or (B) by substitution, i. e. by formally eliminating per constituent compound either two whole groups R1-R7 (as defined) or H, one atom from each of two groups R1-R7 (as defined) or a whole group R1-R7 (as defined) or H and an atom from another group R1-R7 (as defined), and joining the formally so-created valence-unsaturated sites by one covalent bond per constituent compound to provide the same valence as initially present at a given site.
Preferably, the chromium complex has a Cr-Cr-bond or two chromium centres are connected via a bridging ligand.
2007057458 and WO 2007088329. In most of these patents, the obtained mixture of olefins does not contain more than 25 weight-% 1-octene. In some of the most recent applications, different PNP- and similar chelating donor ligands were claimed in conjunction with Cr(III) complexes only (WO 2004/056478 and WO 2004/056479). These applications were the first to demonstrate that in ethylene oligomerization a high selectivity towards 1-octene (up to 70 mass-%) with significantly less simultaneous 1-hexene production can be achieved. It was pointed out that the formed nine-membered ring systems (chromacyclononane) are the reason for the selective tetramerization of ethylene to 1-octene with 70% mass selectivity.
The selective ethylene trimerization and tetramerization catalysts and processes known gener-ally have to cope with some disadvantages. The catalysts show only low selectivities to the desired products 1-hexene and/or 1-octene due to by-products from side reaction channels.
Further limited purities of the products are obtained, i.e. the selectivities within the specific C6- or Cg-cut due to isomerization, branched olefin formation, etc.. Also wax formation, i.e.
formation of heavy, long-chain, high carbon-number products is detected. This is also true for polymer formation (polyethylene, branched and/or cross-linked polyethylene) leading to con-siderable product yield loss and fouling of equipment. Further it has to be mentioned that prior art processes only show poor turnover rates and catalyst activity resulted in high cost per kg product. Prior art catalysts and ligands are usually to be prepared with high costs. Ligands are usually difficult to synthesize, resulting in poor availability and high catalyst cost. The catalyst performance is highly susceptible to trace impurities, and the catalyst components are often difficult to handle in technical environment. The prior art processes usually require harsh reaction conditions, i.e. high temperatures and pressures, resulting in high invest, main-tenance and energy costs. Finally, high costs are also to be expected for co-catalyst/activator.
It is therefore an object of the present invention to overcome the difficulties of the prior art and to provide a catalyst composition showing improved selectivities and purities in the oli-gomerization of ethylene without formation of wax or polymer, showing rather improved turnover rates with fair costs for preparing catalyst and ligand.
Additionally, a process for the oligomerization of ethylene shall be provided.
The first object is achieved by a catalyst composition comprising: (a) a binuclear chro-mium(II) complex; (b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, wherein R1, R2, R3, R4, R5, R6 and R7 are independ-ently selected from halogen, amino, trimethylsilyl, C1-Clo-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system; and (c) an activator or co-catalyst.
As is to be understood, any cyclic derivatives of (A) and (B) can be utilized as ligand, wherein at least one of the P or N atoms of the PNPN-unit (structure (A)) or PNPNP-unit (structure (B)) is a ring member, the ring being formed from one or more constituent com-pounds of structures (A) or (B) by substitution, i. e. by formally eliminating per constituent compound either two whole groups R1-R7 (as defined) or H, one atom from each of two groups R1-R7 (as defined) or a whole group R1-R7 (as defined) or H and an atom from another group R1-R7 (as defined), and joining the formally so-created valence-unsaturated sites by one covalent bond per constituent compound to provide the same valence as initially present at a given site.
Preferably, the chromium complex has a Cr-Cr-bond or two chromium centres are connected via a bridging ligand.
-4-Most preferably, the binuclear chromium complex is selected from:
r\/C \ Cr=------Cr N N
`-- Cr 0, 0-0 O N N
T
O
O 1 I 0- ~ -.
/ O O~>O 10 Cr- Cr Cr-
r\/C \ Cr=------Cr N N
`-- Cr 0, 0-0 O N N
T
O
O 1 I 0- ~ -.
/ O O~>O 10 Cr- Cr Cr-
-5-N L %-1 N N
Cr--- Cr` X
\
N /N
J
Cr--- Cr` X
\
N /N
J
6 C N N
N~N N~N
N Y N N N
C i R! C -N
~cr\\, iY ~O N
In one embodiment, R1, R2, R3, R4, R5, R6 and R7 are selected from chloro, amino, trimethyl-silyl, methyl, ethyl, isopropyl, tert-butyl, phenyl, benzyl, tolyl and xylyl.
N~N N~N
N Y N N N
C i R! C -N
~cr\\, iY ~O N
In one embodiment, R1, R2, R3, R4, R5, R6 and R7 are selected from chloro, amino, trimethyl-silyl, methyl, ethyl, isopropyl, tert-butyl, phenyl, benzyl, tolyl and xylyl.
7 PCT/EP2008/009305 In another embodiment, the activator or co-catalyst is selected from trimethyl aluminium, triethyl aluminium, triisopropylaluminum, triisobutyl aluminium, ethylaluminum sesquichlo-ride, diethylaluminum chloride, ethyl aluminium dichloride, methylaluminoxane (MAO) or mixtures thereof.
The ligand may be selected from (Ph)2P-N(i-Pr)-P(CH3)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(Ph)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(tert-butyl)-H and (Ph)2P-N(i-Pr)-P(Ph)-N(CH(CH3)(Ph))-H.
Preferably, the catalyst composition comprises a solvent, which may be selected from aro-matic hydrocarbons, straight-chain and cyclic aliphatic hydrocarbons, straight-chain olefins and ethers, preferably toluene, benzene, ethyl benzene, cumene, xylenes, mesitylene, hexane, octane, cyclohexane, methylcyclohexane, hexene, heptene, octene, diethylether or tetrahydro-furane or mixtures thereof, most preferably toluene.
A second object of the invention is achieved by a process for oligomerization of ethylene, comprising subjecting a catalyst composition according to the invention to a gas phase of eth-ylene in a reactor and conducting an oligomerization.
Preferably, the oligomerization is carried at a pressure of 1 to 200 bar, preferably 10 to 50 bar.
Also preferred, the oligomerization is carried at a temperature of from 10 to 200 C, preferably 20 to 100 C.
In one embodiment, the process is carried out continuously, semi-continuously or discontinu-ously.
The mean residence time may be from 10 minutes to 20 hours, preferably 1 to 4 hours.
Most preferred, the process is a trimerization or tetramerization.
Surprisingly it was found that a process for oligomerization of ethylene utilizing the inventive catalyst composition avoids the broad spectrum of LAO products and allows for the selective production of the economically most desired products, namely 1-hexene and 1-octene. Unpre-cedented high selectivity, purity and sufficiently high active/turnover frequency are achieved.
The current invention is based on the fact that the selective tetramerization of ethylene to 1-octene and the trimerization of ethylene to 1-hexene can proceed more efficiently by using a binuclear transition metal complex, rather than a mononuclear transition metal complex, whose mechanism involves mononuclear metallocyclononanes and metallacycloheptanes, respectively.
Without wishing to be bound to any theory, it is assumed that for the binuclear chromium complexes utilized in a tetramerization reaction a mechanism is suggested wherein the reac-tion proceeds via metallocyclopentanes which the C4-chain dimerizes to a saturated C8-chain between the metal centers as illustrated in the following scheme:
M IN UM -- UM-MU -- ~~M -~ M M
1-octene The above mechanism is characterized by the novel principle of a dinuclear reductive elimina-tion from chromium(II) via chromium(I) to chromium(O) leading to 1-octene.
The catalyst composition according to the present invention can be tuned by suitable ligands to the novel principle of dinuclear reductive elimination from chromium(O) via chromiuml) to chromium(O) (case: neutral ligands) or from chromium(I)/(II) via chromium(II)/(I) to chro-mium(I)/(0) (case: anionic ligands) leading selectively to 1-hexene:
The ligand may be selected from (Ph)2P-N(i-Pr)-P(CH3)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(Ph)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(tert-butyl)-H and (Ph)2P-N(i-Pr)-P(Ph)-N(CH(CH3)(Ph))-H.
Preferably, the catalyst composition comprises a solvent, which may be selected from aro-matic hydrocarbons, straight-chain and cyclic aliphatic hydrocarbons, straight-chain olefins and ethers, preferably toluene, benzene, ethyl benzene, cumene, xylenes, mesitylene, hexane, octane, cyclohexane, methylcyclohexane, hexene, heptene, octene, diethylether or tetrahydro-furane or mixtures thereof, most preferably toluene.
A second object of the invention is achieved by a process for oligomerization of ethylene, comprising subjecting a catalyst composition according to the invention to a gas phase of eth-ylene in a reactor and conducting an oligomerization.
Preferably, the oligomerization is carried at a pressure of 1 to 200 bar, preferably 10 to 50 bar.
Also preferred, the oligomerization is carried at a temperature of from 10 to 200 C, preferably 20 to 100 C.
In one embodiment, the process is carried out continuously, semi-continuously or discontinu-ously.
The mean residence time may be from 10 minutes to 20 hours, preferably 1 to 4 hours.
Most preferred, the process is a trimerization or tetramerization.
Surprisingly it was found that a process for oligomerization of ethylene utilizing the inventive catalyst composition avoids the broad spectrum of LAO products and allows for the selective production of the economically most desired products, namely 1-hexene and 1-octene. Unpre-cedented high selectivity, purity and sufficiently high active/turnover frequency are achieved.
The current invention is based on the fact that the selective tetramerization of ethylene to 1-octene and the trimerization of ethylene to 1-hexene can proceed more efficiently by using a binuclear transition metal complex, rather than a mononuclear transition metal complex, whose mechanism involves mononuclear metallocyclononanes and metallacycloheptanes, respectively.
Without wishing to be bound to any theory, it is assumed that for the binuclear chromium complexes utilized in a tetramerization reaction a mechanism is suggested wherein the reac-tion proceeds via metallocyclopentanes which the C4-chain dimerizes to a saturated C8-chain between the metal centers as illustrated in the following scheme:
M IN UM -- UM-MU -- ~~M -~ M M
1-octene The above mechanism is characterized by the novel principle of a dinuclear reductive elimina-tion from chromium(II) via chromium(I) to chromium(O) leading to 1-octene.
The catalyst composition according to the present invention can be tuned by suitable ligands to the novel principle of dinuclear reductive elimination from chromium(O) via chromiuml) to chromium(O) (case: neutral ligands) or from chromium(I)/(II) via chromium(II)/(I) to chro-mium(I)/(0) (case: anionic ligands) leading selectively to 1-hexene:
-8-L ~M + C M -- ~M/ M M Z -M
1-hexene Additionally, it was surprisingly found that the modification of a tridentate ligand, such as (phenyl)2P-N(isopropyl)-P(phenyl)2 by an additional NH(isopropyl) unit resulted in the tet-radentate ligand ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)). Utilizing the former ligand in the catalyst composition resulted in a high selectivity towards the tetramerization of ethylene, whereas the latter ligand resulted in a high selectivity for the trimerization or tetramerization of ethylene depending on the substituents, as will be shown below in the ex-amples section.
In other words, the inventive process results in the production of 1-octene and 1-hexene with high turnover rate and selectivity. An easy switchover from 1-octene to 1-hexene production by using specific ligands can be easily obtained. Further, a high reproduceability is obtained, e.g. the catalyst system is stable against interference from impurities and fluctuations in proc-ess conditions. Formation of wax and polymers is well suppressed.
Additionally, in the inven-tive process slight reaction conditions may be employed, consequently resulting in low inves-tive costs for technical-scale plant and low energy and operation costs.
Additional advantages and features of the present invention will become apparent from the following detailed description on the basis of examples.
A ligand to be used in the inventive catalyst composition may be prepared as follows:
1-hexene Additionally, it was surprisingly found that the modification of a tridentate ligand, such as (phenyl)2P-N(isopropyl)-P(phenyl)2 by an additional NH(isopropyl) unit resulted in the tet-radentate ligand ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)). Utilizing the former ligand in the catalyst composition resulted in a high selectivity towards the tetramerization of ethylene, whereas the latter ligand resulted in a high selectivity for the trimerization or tetramerization of ethylene depending on the substituents, as will be shown below in the ex-amples section.
In other words, the inventive process results in the production of 1-octene and 1-hexene with high turnover rate and selectivity. An easy switchover from 1-octene to 1-hexene production by using specific ligands can be easily obtained. Further, a high reproduceability is obtained, e.g. the catalyst system is stable against interference from impurities and fluctuations in proc-ess conditions. Formation of wax and polymers is well suppressed.
Additionally, in the inven-tive process slight reaction conditions may be employed, consequently resulting in low inves-tive costs for technical-scale plant and low energy and operation costs.
Additional advantages and features of the present invention will become apparent from the following detailed description on the basis of examples.
A ligand to be used in the inventive catalyst composition may be prepared as follows:
-9-Preparation of Ph2PN(i-Pr)PMeNH(i-Pr): 2,21 g of Ph2PC1 (10 mmol) was slowly added to a mixture of 1,62 g MeP(NH(i-Pr))2 (10mmol) (Eur. J. Inorg. Chem. 1999, 12, 2355-68) and 5m1 triethylamine in 15 ml toluene at 0 C. The solution was stirred for additional 2h at r.t. and then filtered to remove the amine-hydrochloride. After evaporation of the volatile compounds in vacuo a sticky oil remained. Yield: 80%
31P-NMR (C6D6); 33.7, 57.6 (broad) Trimerization by binuclear complexes Example 1:
Ethylene trimerization using {[(i-Pr)2N]Cr[ -(i-Pr)2N]}2, ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) and triethylaluminum A 300 ml pressure reactor, equipped with dip tube, thermowell, gas entrainment stirrer, cool-ing coil, control units for temperature, pressure and stirrer speed (all hooked up to a data ac-quisition system) was inertized with dry argon and filled with 100 ml anhydrous toluene.
Then 81.7 mg (0.2 mmol) of ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) in
31P-NMR (C6D6); 33.7, 57.6 (broad) Trimerization by binuclear complexes Example 1:
Ethylene trimerization using {[(i-Pr)2N]Cr[ -(i-Pr)2N]}2, ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) and triethylaluminum A 300 ml pressure reactor, equipped with dip tube, thermowell, gas entrainment stirrer, cool-ing coil, control units for temperature, pressure and stirrer speed (all hooked up to a data ac-quisition system) was inertized with dry argon and filled with 100 ml anhydrous toluene.
Then 81.7 mg (0.2 mmol) of ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) in
10 ml tolu-ene was combined with 65.6 mg {[(i-Pr)2N]Cr[ -(i-Pr)2N]}2 (0.13 mmol) under an argon blanket. This catalyst solution was transferred to the reactor under constant argon flow, along with 3.6 ml of a 1.9 mol/l solution of triethylaluminium in toluene.
The reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. While stir-ring at 1200 rpm, the ethylene consumption was monitored by the data acquisition system and an electronic balance by constantly weighing the ethylene pressure cylinder. After 120 min residence time, the reaction in the liquid phase was quenched by transferring the liquid inventory by means of the ethylene pressure to a glass vessel filled with approx. 100 ml of water. The entire gas phase from the reactor's head space was quantified by a calibrated gas meter and was then collected quantitatively in a purged and evacuated gas bag.
After separation of the liquid organic phase, the total mass was determined by weighing. Sub-sequently, the composition of the organic phase was analyzed separately by GC/FID. Based on the measured data, the mass balance was closed and the overall yields and selectivities were determined. The product distribution of this example is summarized in Table 1.
Comparative Example 2:
Ethylene trimerization using CrC13(tetrahydrofurane)3, ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene.
A solution of 81.7 mg (0.2 mmol) of ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) in 10 ml toluene was combined with 50.0 mg (0.13 mmol) CrC13(tetrahydrofuran)3 under a argon blanket. This catalyst solution was transferred to the reactor along with 3.6 ml of a 1.9 mol/l solution of triethlaluminium in toluene. The reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the re-action mixture was worked up and analyzed as mentioned above. The product distribution of this example is summarized in Table 1.
The comparison shows higher activity for binuclear complexes.
Table 1. Ethylene trimerization runs Example Activity, kg C6-Yield, wt% Cg-Yield, wt% 1-hex in C6 prod./g Cr 1 145 88 1 99.0 2 34 89 1 99.0 Tetramerization by binuclear compounds
The reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. While stir-ring at 1200 rpm, the ethylene consumption was monitored by the data acquisition system and an electronic balance by constantly weighing the ethylene pressure cylinder. After 120 min residence time, the reaction in the liquid phase was quenched by transferring the liquid inventory by means of the ethylene pressure to a glass vessel filled with approx. 100 ml of water. The entire gas phase from the reactor's head space was quantified by a calibrated gas meter and was then collected quantitatively in a purged and evacuated gas bag.
After separation of the liquid organic phase, the total mass was determined by weighing. Sub-sequently, the composition of the organic phase was analyzed separately by GC/FID. Based on the measured data, the mass balance was closed and the overall yields and selectivities were determined. The product distribution of this example is summarized in Table 1.
Comparative Example 2:
Ethylene trimerization using CrC13(tetrahydrofurane)3, ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene.
A solution of 81.7 mg (0.2 mmol) of ((phenyl)2PN(isopropyl)P(phenyl)NH(isopropyl)) in 10 ml toluene was combined with 50.0 mg (0.13 mmol) CrC13(tetrahydrofuran)3 under a argon blanket. This catalyst solution was transferred to the reactor along with 3.6 ml of a 1.9 mol/l solution of triethlaluminium in toluene. The reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the re-action mixture was worked up and analyzed as mentioned above. The product distribution of this example is summarized in Table 1.
The comparison shows higher activity for binuclear complexes.
Table 1. Ethylene trimerization runs Example Activity, kg C6-Yield, wt% Cg-Yield, wt% 1-hex in C6 prod./g Cr 1 145 88 1 99.0 2 34 89 1 99.0 Tetramerization by binuclear compounds
-11-Example 3:
Ethylene tetramerization using {[(i-Pr)2N]Cr[.t-(i-Pr)2N]}2i ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene and a solution of 69.3 mg of ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) (0.2 mmol) in ml toluene together with 65.6 mg {[(i-Pr)2N]Cr[ -(i-Pr)2N]}2 (0.13 mmol).
After adding 3.6 ml of a 1.9 M solution of triethylaluminum in toluene the reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the reaction mixture was worked up and analyzed as mentioned above.
The product distribution of this example is summarized in Table 2.
Comparative Example 4:
Ethylene oligomerization using CrC13(tetrahydrofuran)3, ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene and a solution of 69.3 mg of ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) (0.2 mmol) in 10 ml toluene together with 50.0 mg CrC13(tetrahydrofuran)3 (0.13 mmol). After adding 3.6 ml of a 1.9 M solution of triethylaluminum in toluene the reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the reaction mixture was worked up and analyzed as mentioned above. The product dis-tribution of this example is consistent with a Schulz-Flory distribution and summarized in Table 2.
Table 2. Ethylene tetramerization runs
Ethylene tetramerization using {[(i-Pr)2N]Cr[.t-(i-Pr)2N]}2i ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene and a solution of 69.3 mg of ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) (0.2 mmol) in ml toluene together with 65.6 mg {[(i-Pr)2N]Cr[ -(i-Pr)2N]}2 (0.13 mmol).
After adding 3.6 ml of a 1.9 M solution of triethylaluminum in toluene the reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the reaction mixture was worked up and analyzed as mentioned above.
The product distribution of this example is summarized in Table 2.
Comparative Example 4:
Ethylene oligomerization using CrC13(tetrahydrofuran)3, ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) and triethylaluminum In analogy to Example 1 a 300 ml pressure reactor was filled with 100 ml anhydrous toluene and a solution of 69.3 mg of ((phenyl)2PN(isopropyl)P(methyl)NH(isopropyl)) (0.2 mmol) in 10 ml toluene together with 50.0 mg CrC13(tetrahydrofuran)3 (0.13 mmol). After adding 3.6 ml of a 1.9 M solution of triethylaluminum in toluene the reactor was sealed, pressurized with 30 bar dry ethylene and heated to 50 C. After 120 min residence time while stirring at 1200 rpm the reaction mixture was worked up and analyzed as mentioned above. The product dis-tribution of this example is consistent with a Schulz-Flory distribution and summarized in Table 2.
Table 2. Ethylene tetramerization runs
-12-Example Activity, kg C6-Yield, C8-Yield, 1-hex in C6 1-oct in C8 prod./g Cr wt% wt%
3 21 8 82 98.0 98.0 4 33 30 28 98.0 98.0 As can be seen from the examples, by changing the ligand utilized in the catalyst composition an easy switch from trimerization (Example 1 and 2) to tetramerization (Example 3) may be achieved. Furthermore by using binuclear chromium(II) complexes an easy switch from unse-lective oligomerization (Example 4) to tetramerization (Example 3) is possible.
The features disclosed in the foregoing description and in the claims may, both separately and in any combination thereof, be material for realizing the invention in diverse forms thereof.
3 21 8 82 98.0 98.0 4 33 30 28 98.0 98.0 As can be seen from the examples, by changing the ligand utilized in the catalyst composition an easy switch from trimerization (Example 1 and 2) to tetramerization (Example 3) may be achieved. Furthermore by using binuclear chromium(II) complexes an easy switch from unse-lective oligomerization (Example 4) to tetramerization (Example 3) is possible.
The features disclosed in the foregoing description and in the claims may, both separately and in any combination thereof, be material for realizing the invention in diverse forms thereof.
Claims (13)
1. Catalyst composition comprising:
(a) a binuclear chromium(II) complex;
(b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, wherein R1, R2, R3, R4, R5, R6 and R7 are independently selected from halogen, amino, trimethylsilyl, C1-C10-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system;
and (c) an activator or co-catalyst.
(a) a binuclear chromium(II) complex;
(b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, wherein R1, R2, R3, R4, R5, R6 and R7 are independently selected from halogen, amino, trimethylsilyl, C1-C10-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system;
and (c) an activator or co-catalyst.
2. Catalyst composition according to claim 1, wherein the chromium complex has a Cr-Cr-bond or two chromium centers are connected via a bridging ligand.
3. Catalyst composition according to any of the preceding claims, wherein the binuclear chromium complex is selected from:
4. Catalyst composition according to any of the preceding claims, wherein R1, R2, R3, R4, R5, R6 and R7 are selected from chloro, amino, trimethylsilyl, methyl, ethyl, isopropyl, tert-butyl, phenyl, benzyl, tolyl and xylyl.
5. Catalyst composition according to any of the preceding claims, wherein the activator or co-catalyst is selected from trimethyl aluminium, triethyl aluminium, triisopropyl aluminum, triisobutyl aluminium, ethylaluminum sesquichloride, diethylaluminum chloride, ethyl aluminium dichloride, methylaluminoxane (MAO) or mixtures thereof.
6. Catalyst composition according to any of the preceding claims, wherein the ligand is selected from (Ph)2P-N(i-Pr)-P(CH3)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(i-Pr)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(Ph)-H, (Ph)2P-N(i-Pr)-P(Ph)-N(tert-butyl)-H and (Ph)2P-N(i-Pr)-P(Ph)-N(CH(CH3)(Ph))-H.
7. Catalyst composition according to any of the preceding claims additionally comprising a solvent.
8. Catalyst composition according to claim 7, wherein the solvent is selected from aro-matic hydrocarbons, straight-chain and cyclic aliphatic hydrocarbons, straight-chain olefins and ethers, preferably toluene, benzene, ethyl benzene, cumene, xylenes, me-sitylene, hexane, octane, cyclohexane, methylcyclohexane, hexene, heptene, octene, diethylether or tetrahydrofurane or mixtures thereof, most preferably toluene.
9. Process for oligomerization of ethylene, comprising subjecting a catalyst composition according to any of the claims 1 to 8 to a gas phase of ethylene in a reactor and con-ducting an oligomerization at a temperature of from 20 to 100°C.
10. Process according to claim 9, wherein the oligomerization is carried at a pressure of 1 to 200 bar, preferably 10 to 50 bar.
11. Process according to claim 9 or 10, wherein the process is carried out continuously.
12. Process according to any of the claims 9 to 11, wherein the mean residence time is from 10 minutes to 20 hours, preferably 1 to 4 hours.
13. Catalyst composition, obtainable by combining at least:
(a) a binuclear chromium(II) complex;
(b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, Wherein R1, R2, R3, R4, R5, R6 and R7 are independently selected from halogen, amino, trimethylsilyl, C1-C10-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system;
and (c) an activator or co-catalyst.
(a) a binuclear chromium(II) complex;
(b) a ligand of the general structure (A) R1R2P-N(R3)-P(R4)-N(R5)-H or (B) R1R2P-N(R3)-P(R4)-N(R5)-PR6R7, Wherein R1, R2, R3, R4, R5, R6 and R7 are independently selected from halogen, amino, trimethylsilyl, C1-C10-alkyl, aryl and substituted aryl, wherein the PNPN- or PNPNP-unit is optionally part of a ring system;
and (c) an activator or co-catalyst.
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| PCT/EP2008/009305 WO2009068157A1 (en) | 2007-11-28 | 2008-11-05 | Catalyst composition and process for oligomerization of ethylene |
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| JP5013173B2 (en) | 2005-11-22 | 2012-08-29 | 株式会社豊田中央研究所 | Organometallic complex, occlusion material and catalyst using the same |
| CN101415494A (en) | 2006-02-03 | 2009-04-22 | 英尼奥斯欧洲有限公司 | Transition metal catalysts |
| US8637721B2 (en) * | 2007-07-11 | 2014-01-28 | Saudi Basic Industries Corporation | Catalyst composition and process for di-, tri- and/or tetramerization of ethylene |
| MX2010005266A (en) | 2007-11-28 | 2010-06-02 | Linde Ag | Catalyst composition and process for oligomerization of ethylene. |
-
2008
- 2008-11-05 MX MX2010005266A patent/MX2010005266A/en active IP Right Grant
- 2008-11-05 US US12/734,770 patent/US8778827B2/en not_active Expired - Fee Related
- 2008-11-05 CA CA2703021A patent/CA2703021C/en not_active Expired - Fee Related
- 2008-11-05 KR KR1020107009317A patent/KR101445431B1/en active IP Right Grant
- 2008-11-05 ES ES08855368T patent/ES2397303T3/en active Active
- 2008-11-05 WO PCT/EP2008/009305 patent/WO2009068157A1/en active Application Filing
- 2008-11-05 JP JP2010535257A patent/JP5462179B2/en not_active Expired - Fee Related
- 2008-11-05 BR BRPI0819904-3A patent/BRPI0819904B1/en not_active IP Right Cessation
- 2008-11-05 RU RU2010126183/04A patent/RU2467797C2/en active
- 2008-11-05 MY MYPI20101804 patent/MY150515A/en unknown
- 2008-11-05 CN CN2008801154457A patent/CN101855015B/en not_active Expired - Fee Related
- 2008-11-05 EP EP08855368A patent/EP2219784B1/en not_active Not-in-force
- 2008-11-14 TW TW097144266A patent/TWI440503B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100088665A (en) | 2010-08-10 |
| US20100298618A1 (en) | 2010-11-25 |
| TWI440503B (en) | 2014-06-11 |
| CN101855015B (en) | 2013-07-17 |
| JP5462179B2 (en) | 2014-04-02 |
| EP2219784B1 (en) | 2012-10-24 |
| JP2011504799A (en) | 2011-02-17 |
| WO2009068157A1 (en) | 2009-06-04 |
| US8778827B2 (en) | 2014-07-15 |
| EP2219784A1 (en) | 2010-08-25 |
| BRPI0819904A2 (en) | 2015-09-15 |
| RU2467797C2 (en) | 2012-11-27 |
| MY150515A (en) | 2014-01-30 |
| CN101855015A (en) | 2010-10-06 |
| CA2703021C (en) | 2015-01-20 |
| MX2010005266A (en) | 2010-06-02 |
| KR101445431B1 (en) | 2014-09-26 |
| TW200942327A (en) | 2009-10-16 |
| RU2010126183A (en) | 2012-01-10 |
| BRPI0819904B1 (en) | 2018-02-06 |
| ES2397303T3 (en) | 2013-03-06 |
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